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NCT ID: NCT01272752 Withdrawn - Obesity Clinical Trials

Anti-psychotic Medication (New Use) Weight Loss Study

Start date: April 2013
Phase: Phase 2
Study type: Interventional

This is a pilot study to determine the safety and efficacy of an investigational product (IHBG-10) on weight change and changes in body composition in subjects who have just started taking (for less than three months) certain anti-psychotic medications (Risperdal, Seroquel, and/or Zyprexa).

NCT ID: NCT01331655 Withdrawn - Contraception Clinical Trials

Clinical Study of a Conventional and Flexible Extended Oral Contraceptive of EE/DRSP With or Without Metafolin in Latin America

Start date: April 2013
Phase: Phase 3
Study type: Interventional

The objective of this three-arm study is to evaluate the effect of a flexible extended regimen of an EE+DRSP containing OC on bleeding pattern and to investigate the compliance with daily pill intake when the investigational product is provided in a blister package or a compliance aiding dispenser with a pill reminder function. The third treatment arm will be a reference comparator arm of a standard 24+4 regimen of the identical hormone combination.

NCT ID: NCT01359228 Withdrawn - Rosacea Clinical Trials

Rifaximin Treatment of Papulopustular Rosacea

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effects of rifaximin on skin symptoms in patients with rosacea by double-blinded, placebo-controlled, crossover study.

NCT ID: NCT01461252 Withdrawn - Pain Clinical Trials

Safety and Efficacy of Cryoablation Combined With Radiation Therapy for the Palliation of Painful Bone Metastases

Start date: April 2013
Phase: Phase 1
Study type: Interventional

This study will evaluate the safety and efficacy of cryoablation therapy combined with radiation therapy for the relief of pain associated with metastatic bone tumors.

NCT ID: NCT01521442 Withdrawn - PTSD Clinical Trials

Mindful Yoga Therapy as an Adjunctive Treatment for PTSD Among OEF/OIF Veterans

Start date: April 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective of the current study is to establish the safety and acceptability of Mindful Yoga Therapy as an adjunctive treatment for posttraumatic stress disorder (PTSD) among Operation Enduring Freedom/Operation Iraqi Freedom/Operation New Dawn (OEF/OIF/OND) Veterans. The current study also seeks to establish preliminary efficacy of Mindful Yoga Therapy for reduction of symptoms of PTSD and explore heart rate variability as a mechanism of therapeutic action.

NCT ID: NCT01538992 Withdrawn - Heart Failure Clinical Trials

Renal Denervation in Patients With Advanced Heart Failure

Start date: April 2013
Phase: Phase 3
Study type: Interventional

Sympathetic system has important role occurrence of symptoms in heart failure. Renal denervation that is ablated some of sympathetic nerves is affected pathology of heart failure. This interventional therapy improves symptoms and life quality.

NCT ID: NCT01551537 Withdrawn - Clinical trials for Human Papillomavirus Infection

Post-marketing Surveillance of GSK Biologicals' Cervarix™ When Administered to Healthy Females in Sri Lanka

Start date: April 2013
Phase: N/A
Study type: Observational

This PMS study aims to collect safety and reactogenicity data of Cervarix in the local population as per the licensing requirement of the Sri Lankan regulatory authority.

NCT ID: NCT01674868 Withdrawn - Stroke Clinical Trials

Fluoxetine for Motor, Aphasia, and Neglect Recovery After Ischemic Stroke

FLAN
Start date: April 2013
Phase: N/A
Study type: Interventional

This pilot study will recruit 25 subjects to assess the feasibility of replicating the FLAME study (Chollet, et al. Lancet 2011), a randomized controlled trial (RCT) that assessed the effect of fluoxetine vs placebo on motor recovery after ischemic stroke, in an American sample of post-acute stroke patients. This trial will in addition examine the effect of treatment with fluoxetine versus placebo on concurrent deficits in language and hemispatial attention, as well as post-stroke fatigue and will evaluate the durability of observed effects. The results of this pilot trial will be used to develop power estimates for a larger trial and to evaluate recruitment and intervention completion rates for subjects in an American post-acute environment. There are two additional substudies: the first will use MRI to assess structural changes at the beginning and end of the intervention; the second will examine the relationship of serum biomarkers of inflammation to the intervention.

NCT ID: NCT01691963 Withdrawn - Clinical trials for Intubation Complication

Epiglottic Downfolding During Endotracheal Intubation

Start date: April 2013
Phase: N/A
Study type: Interventional

Usually videolaryngoscopy using a videolaryngoscope with a classic Macintosh design is performed with the blade in the vallecula and the epiglottis elevated from the vocal cords indirectly, as in direct laryngoscopy. However, during an audit of videolaryngoscopic practice we noticed that, in obtaining the best view, clinicians frequently and inadvertently advanced the blade into the vallecula to get a better view, such that the epiglottis was downfolded and elevated directly from the vocal cords. However, a better view does not necessarily lead to higher intubation success. In this randomized, controlled trial, we want to determine the efficacy of videolaryngoscope-guided tracheal intubation using an alternative position for the blade in patients with normal airways.

NCT ID: NCT01718704 Withdrawn - Clinical trials for Erectile Dysfunction Following Radical Prostatectomy

Viberect Penile Vibratory Stimulation to Enhance Recovery of Erectile Function and Urinary Continence Post-Prostatectomy

Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether using penile vibratory stimulation with the Viberect handheld device can help the recovery of erections and urinary control after radical prostatectomy.